Canonical Allele Identifier: CA003625

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 91653
• ClinVar RCV Id: RCV000077170 ; RCV000637422 ; RCV001024146
• dbSNP Id: rs398122699
• MyVariant Identifiers: chr17:g.41197821T>C (hg19) ; chr17:g.43045804T>C (hg38)
• PubMed: PMID:26028024

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43045804T>C , CM000679.2:g.43045804T>C	GRCh38
NC_000017.10:g.41197821T>C , CM000679.1:g.41197821T>C	GRCh37
NC_000017.9:g.38451347T>C	NCBI36
NG_005905.2:g.172180A>G , LRG_292:g.172180A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5465-2A>G	ENSP00000417241.2:n.5465-2A>G
ENST00000470026.6:c.5468-2A>G	ENSP00000419274.2:n.5468-2A>G
ENST00000473961.6:c.5342-2A>G	ENSP00000420201.2:n.5342-2A>G
ENST00000476777.6:c.5462-2A>G	ENSP00000417554.2:n.5462-2A>G
ENST00000477152.6:c.5390-2A>G	ENSP00000419988.2:n.5390-2A>G
ENST00000478531.6:c.2156-2A>G	ENSP00000420412.2:n.2156-2A>G
ENST00000489037.2:c.5390-2A>G	ENSP00000420781.2:n.5390-2A>G
ENST00000493919.6:c.2018-2A>G	ENSP00000418819.2:n.2018-2A>G
ENST00000494123.6:c.5468-2A>G	ENSP00000419103.2:n.5468-2A>G
ENST00000497488.2:c.4580-2A>G	ENSP00000418986.2:n.4580-2A>G
ENST00000618469.2:c.5468-2A>G	ENSP00000478114.2:n.5468-2A>G
ENST00000634433.2:c.5345-2A>G	ENSP00000489431.2:n.5345-2A>G
ENST00000644379.2:c.5534-2A>G	ENSP00000496570.2:n.5534-2A>G
ENST00000644555.2:c.2018-2A>G	ENSP00000494614.2:n.2018-2A>G
ENST00000652672.2:c.5327-2A>G	ENSP00000498906.2:n.5327-2A>G
ENST00000484087.6:c.2030-2A>G	ENSP00000419481.2:n.2030-2A>G
ENST00000700081.1:n.1351-2A>G
ENST00000700082.1:n.832-2A>G
ENST00000357654.9:c.5468-2A>G MANE Select	ENSP00000350283.3:n.5468-2A>G
ENST00000471181.7:c.5531-2A>G	ENSP00000418960.2:n.5531-2A>G
ENST00000644379.1:c.1855-2A>G
ENST00000352993.7:c.2042-2A>G	ENSP00000312236.5:n.2042-2A>G
ENST00000357654.7:c.5468-2A>G	ENSP00000350283.3:n.5468-2A>G
ENST00000461221.5:c.*5251-2A>G	ENSP00000418548.1:n.*5251-2A>G
ENST00000468300.5:c.2082-2A>G	ENSP00000417148.1:n.2082-2A>G
ENST00000471181.6:c.5531-2A>G	ENSP00000418960.2:n.5531-2A>G
ENST00000491747.6:c.2156-2A>G	ENSP00000420705.2:n.2156-2A>G
ENST00000493795.5:c.5327-2A>G	ENSP00000418775.1:n.5327-2A>G
ENST00000586385.5:c.398-2A>G	ENSP00000465818.1:n.398-2A>G
ENST00000591534.5:c.941-2A>G	ENSP00000467329.1:n.941-2A>G
ENST00000591849.5:c.167-2A>G	ENSP00000465347.1:n.167-2A>G
NM_007294.3:c.5468-2A>G , LRG_292t1:c.5468-2A>G	NP_009225.1:n.5468-2A>G
NM_007297.3:c.5327-2A>G	NP_009228.2:n.5327-2A>G
NM_007298.3:c.2156-2A>G	NP_009229.2:n.2156-2A>G
NM_007299.3:c.2082-2A>G	NP_009230.2:n.2082-2A>G
NM_007300.3:c.5531-2A>G	NP_009231.2:n.5531-2A>G
NR_027676.1:n.5604-2A>G
NM_007294.4:c.5468-2A>G MANE Select	NP_009225.1:n.5468-2A>G
NM_007297.4:c.5327-2A>G	NP_009228.2:n.5327-2A>G
NM_007299.4:c.2082-2A>G	NP_009230.2:n.2082-2A>G
NM_007300.4:c.5531-2A>G	NP_009231.2:n.5531-2A>G
NR_027676.2:n.5645-2A>G